HCID 22407359, compound → HCID 22407555, compound

HRID 440588Notes

Reaction equation

HRID 440588 reaction equation
[CH2:1]([C:5]1[NH:6][C:7]2[C:12]([C:13](=[O:15])[N:14]=1)=[CH:11][CH:10]=[CH:9][C:8]=2[CH3:16])[CH2:2][CH2:3][CH3:4].[CH2:17]([O:19][C:20]([CH:22]([O:29][C:30]1[CH:37]=[CH:36][C:33]([CH2:34]Br)=[CH:32][CH:31]=1)[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)=[O:21])[CH3:18]>>[CH2:1]([C:5]1[N:14]([CH2:34][C:33]2[CH:36]=[CH:37][C:30]([O:29][CH:22]([C:20]([O:19][CH2:17][CH3:18])=[O:21])[C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)=[CH:31][CH:32]=2)[C:13](=[O:15])[C:12]2[C:7](=[C:8]([CH3:16])[CH:9]=[CH:10][CH:11]=2)[N:6]=1)[CH2:2][CH2:3][CH3:4]

Participants

3

Reactant 2

HCID 22407359HCID 22407359, compoundHCID 178441838HCID 178441838, compound

Product 1

HCID 22407555HCID 22407555, compound

Procedure

Prepared analogously to Example 1a from 2-n-butyl-8-methyl-quinazolin-4(1H)-one and 4-(α-ethoxycarbonylbenzyloxy)benzylbromide.

Sources & evidence

ORD record
ord-c96d26258ae440c79af93ba4e4fa9d5b
Source dataset
uspto-grants-1996_05
Patent number
US05519138

Reaction notes

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